Purification, crystallization and preliminary x-ray crystallographic studies of RAIDD Death-Domain (DD)

Int J Mol Sci. 2009 Jun 3;10(6):2501-2509. doi: 10.3390/ijms10062501.

Abstract

Caspase-2 activation by formation of PIDDosome is critical for genotoxic stress induced apoptosis. PIDDosome is composed of three proteins, RAIDD, PIDD, and Caspase-2. RAIDD is an adaptor protein containing an N-terminal Caspase-Recruiting-Domain (CARD) and a C-terminal Death-Domain (DD). Its interactions with Caspase-2 and PIDD through CARD and DD respectively and formation of PIDDosome are important for the activation of Caspase-2. RAIDD DD cloned into pET26b vector was expressed in E. coli cells and purified by nickel affinity chromatography and gel filtration. Although it has been known that the most DDs are not soluble in physiological condition, RAIDD DD was soluble and interacts tightly with PIDD DD in physiological condition. The purified RAIDD DD alone has been crystallized. Crystals are trigonal and belong to space group P3(1)21 (or its enantiomorph P3(2)21) with unit-cell parameters a = 56.3, b = 56.3, c = 64.9 A and gamma = 120 degrees . The crystals were obtained at room temperature and diffracted to 2.0 A resolution.

Keywords: Death-Domain (DD); PIDDosome; RAIDD; crystallization.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • CRADD Signaling Adaptor Protein / chemistry*
  • CRADD Signaling Adaptor Protein / genetics
  • CRADD Signaling Adaptor Protein / isolation & purification
  • Chromatography, Affinity
  • Cloning, Molecular
  • Crystallography, X-Ray
  • Humans
  • Protein Structure, Tertiary
  • Recombinant Proteins / biosynthesis
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / isolation & purification

Substances

  • CRADD Signaling Adaptor Protein
  • CRADD protein, human
  • Recombinant Proteins